Synthesis of 3:2 mullite ceramics from silica-enriched filter cake waste via diphasic gels method

Read full text
Authors: Ermias Abebe Negash, Getinet Asrat Mengesha, Belay Brehane Tesfamariam, Tamirat Addis, Yeabsira Sisay Mekuriya, Sena Tadesse Beyene
Cited by: 1
References: 68

Abstract

Mullite ceramics were synthesized from filter cake waste following the diphasic gel method. Filter cake waste, with over 65% silica content, and aluminum nitrate nonahydrate were utilized as the sources of silica and alumina, respectively. The prepared samples were sintered at various temperatures of 1150, 1250, and 1350 °C. The sintered bodies were then evaluated for porosity, density, compressive strength, and dielectric strength. Differential Thermal Analysis (DTA) revealed exothermic peaks at 970 °C and 1147 °C, corresponding to spinel and mullite formation, which was also confirmed by X-ray diffraction (XRD) analysis. The XRD result also showed single-phase mullite crystallization at 1250 °C. Field Emission-Scanning Electron Microscopy (FESEM) and Energy Dispersive Spectroscopy (EDS) demonstrated morphological changes, grain growth, and uniform elemental distribution in sintered mullite ceramics. The mullite ceramics sintered at 1350 °C exhibited a density of 2.615 g/cm 3 , compressive strength of 420 MPa, and dielectric strength of 10.2 kV/mm. These findings highlight the potential of the diphasic gel method to produce high-quality mullite ceramics from industrial waste, contributing to cost-effective, eco-friendly materials with promising applications, including electronic devices, electrical power transmission systems, and other structural and functional advanced ceramics.

Fields of Study & Subjects

Advanced ceramic materials synthesis Recycling and utilization of industrial and municipal waste in materials production Nuclear materials and radiation effects

Publication details

Journal / source
Scientific Reports
Publisher
Springer Science and Business Media LLC
Volume
16
Issue
1
Pages
5150–5150
Publication date
13 January 2026
Language
EN